Evolutionary Understanding of Aquaporin Transport System in the Basal Eudicot Model Species Aquilegia coerulea

• Published in: Plants (Basel) 2020-06, Vol.9 (6), p.799
• Main Authors: Singh, Shweta, Bhatt, Vacha, Kumar, Virender, Kumawat, Surbhi, Khatri, Praveen, Singla, Pankaj, Shivaraj, S.M., Nadaf, Altaf, Deshmukh, Rupesh, Sharma, Tilak Raj, Sonah, Humira
• Format: Article
• Language: English
• Subjects: Alanine; Aquaporins; Aquilegia; Aquilegia coerulea; Arginine; Asparagine; Bioinformatics; Cell division; Comparative analysis; Evolution; Flowers & plants; Gene expression; Genomes; Identification; Localization; Morphology; Nectar; NPA motifs; Phylogenetics; Phylogeny; Physiology; Poplar; Proline; Protein structure; Proteins; Ribonucleic acid; RNA; Selectivity; Servers; Software; Solutes; Structural analysis; transcriptomics; Transportation systems; transporter; Trees
• ISSN: 2223-7747; 2223-7747
• DOI: 10.3390/plants9060799

Aquaporins (AQPs) play a pivotal role in the cellular transport of water and many other small solutes, influencing many physiological and developmental processes in plants. In the present study, extensive bioinformatics analysis of AQPs was performed in Aquilegia coerulea L., a model species belonging to basal eudicots, with a particular focus on understanding the AQPs role in the developing petal nectar spur. A total of 29 AQPs were identified in Aquilegia, and their phylogenetic analysis performed with previously reported AQPs from rice, poplar and Arabidopsis depicted five distinct subfamilies of AQPs. Interestingly, comparative analysis revealed the loss of an uncharacterized intrinsic protein II (XIP-II) group in Aquilegia. The absence of the entire XIP subfamily has been reported in several previous studies, however, the loss of a single clade within the XIP family has not been characterized. Furthermore, protein structure analysis of AQPs was performed to understand pore diversity, which is helpful for the prediction of solute specificity. Similarly, an AQP AqcNIP2-1 was identified in Aquilegia, predicted as a silicon influx transporter based on the presence of features such as the G-S-G-R aromatic arginine selectivity filter, the spacing between asparagine-proline-alanine (NPA) motifs and pore morphology. RNA-seq analysis showed a high expression of tonoplast intrinsic proteins (TIPs) and plasma membrane intrinsic proteins (PIPs) in the developing petal spur. The results presented here will be helpful in understanding the AQP evolution in Aquilegia and their expression regulation, particularly during floral development.